Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:52705781-52706227 | Common:2; Rare:155 | ||||
chr3:53130405-53130533 | Common:1; Rare:40; Clinvar (benign):3 | ||||
chr3:53255959-53256204 | Common:3; Rare:104 | ||||
chr3:53347521-53347741 | Common:1; Rare:68 | ||||
chr3:53891802-53892035 | Common:2; Rare:71 | ||||
chr3:56557086-56557228 | Common:2; Rare:54 | ||||
chr3:57597331-57597661 | Common:4; Rare:104 | ||||
chr3:62318890-62319049 | Rare:67 | ||||
chr3:63863747-63864114 | Common:7; Rare:120 | ||||
chr3:67654587-67654727 | Common:1; Rare:51 | ||||
chr3:69013590-69013750 | Rare:42 | ||||
chr3:69084754-69085050 | Common:3; Rare:73 | ||||
chr3:72996712-72997038 | Common:2; Rare:122 | ||||
chr3:81761630-81761796 | Common:2; Rare:54; Clinvar:1 | ||||
chr3:88058942-88059282 | Common:2; Rare:116 |